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Topped last week plants are growing vigorous Day 58 is today 06/01/21 today I topped dressed with 4-4-4 and earthworm castings and continue to lst plants

Week 1 she is up!

Second week of flowering in the bag, and they’re all looking really healthy, even healthier than when I first threw them in the flower steady as she goes

Der Stretch geht langsam so richtig los, die guten ladies haben 25cm in der letzten Woche dazu gewonnen, ein bisschen geht da aber noch :D Samstag wurde gelollipopt

Greetings fellow growers 🖖 and welcome to my first grow ever. This adventure actually started several months ago when I decided to stop buying flower from dispensaries and just grow my own bud. How hard can it be!? This is actually my second seed of this strain. The first bean sadly died due to over watering (sorry girl, RIP). I was literally watering the cube to the point where water was dripping from the bottom, then heavily sprayed the humidity dome and tray with the vents completely closed. Everyday. Multiple times. I never let the dome or try dry out. So after about 8 days of not sprouting, there was a funky smell of rot. So that was that. Later I learned that rockwool retains a lot of water and can easily drown seeds. So a wet/dry cycle is best for rockwool germination. So even after hours of researching and digging through forums and tutorial videos, I was still under prepared for this journey. Did not consider how delicate the germination phase is. Oh well. Lesson learned. Reset and try again! I hope everyone is safe and stoned during this corona crisis. Just like everyone else in the world, I want this pandemic to be over with. But in the meantime, let's grow some weed! 🖖 [START OF WEEK 01] Day 01 - Monday - 08/03/20 - Total Days: 001 ----------------------------------- - [0830]: Light Schedule: 24Hrs/0 --- Soaked cube in 5.5 PH water for 10 min. Did not shake water out. --- NO NUTES! Only PH'd down to control the PH levels. --- Did not use the default hole (way too deep). --- Flipped cube upside down and made a shallow hole for the seed (less than 0.25" deep). --- Placed seed in and pinched hole close. No additional water added. --- Sprayed the tray and dome with straight water (5.5 PH). --- Vents are cracked opened a for ventilation (about 1/4 opened each). --- Distance between the light and tray was 53" --- AC was set to 80 °F --- Exhaust fan was set to 86 °F --- Room average temp was at 85 °F --- Dome humidity was at 85-99% when sprayed. --- Allowing to completely dry before respraying. - [2200]: Dome and tray were completely dry! Sprayed only tray and dome with more water. Day 02 - Tuesday - 08/04/20 - Total Days: 002 ----------------------------------- - [0845]: Sprayed dome and tray in the morning. Everything was dry. --- Hoping for the best! - [2130]: Everything was dry again, so sprayed dome and tray at night along with a light spray on the cube. Day 03 - Wednesday - 08/05/20 - Total Days: 003 ----------------------------------- - [0830]: Everything was dry again. Resprayed dome and tray. Slightly sprayed cube. - [2125]: Hooo damn!! She popped! Am little stub is visible! Resprayed dome and tray again. --- Still going 24/0 for lights. - [+0033]: Just checked up on her and I swear she grew a bit taller! Getting excited! Day 04 - Thursday - 08/06/20 - Total Days: 004 ----------------------------------- - [0845]: Wow! Went from a little stub to fully sprouted overnight! Everything was pretty dry again so resprayed dome and tray. - [2200]: Tap root is visible! Over 1" long too! Just resprayed dome and tray again. -- Going to prep for hydroton transplant tomorrow! Day 05 - Friday - 08/07/20 - Total Days: 005 ----------------------------------- - [0930]: She keeps growing! -- Added a bit of CalMag to the spray bottle (8 drops to 650ml of distilled water). Resprayed dome and tray. Water was at a 5.4 PH with 141 PPM. - [1045]: Prepped the bubble bucket with 4.5gal of water. Water is high enough to reach about 0.25" above the bottom of the net pot. --- Added 3 drops of Superthrive --- Added 3.5ml of CaliMagic --- Added 2ml Hydroguard --- Then PH'd down to 5.6 --- Solution Strengh: 120 PPM --- Water chiller is set to 20 °C - [1100]: Transplant time! --- Filled the net basket 1/3 with hydroton. When placed in the bucket, air bubbles are not visible, but are slightly below the surface (slight digging will reveal the water/bubbles below). --- Removed plastic on rockwool cube and placed in basket, then filled around and covered with hydroton. Making sure to block any light from passing through the net pot and into the nutrient solution. --- Covered with a half-bottle dome sprayed with the CalMag water from earlier. --- Hoping for the best! - [1300]: Raised Bucket 5" higher. Now light distance is 48" to top of bucket. - [1820]: Lowered tent exhaust temp to 76 °F --- Lowered AC to 75 °F --- Raised bucket even higher so light distance is 30" to top of bucket. - [2300]: Looking good! --- Sprayed dome and surrounding hydroton with more CalMag water. --- Attached timer to light! So new 18 Hrs On/6 Hrs Off light schedule. --- Lights On: [1600] (4pm) --- Lights Off: [+1000] (10am the next day) --- Decided to go with lights on during the evening/night and off during the later mornings/afternoon (the hottest part of the day) to see if temps can be controlled better. --- Please survive girl! Day 06 - Saturday - 08/08/20 - Total Days: 006 ----------------------------------- - [0800]: Everything was dry. Resprayed hydroton and dome. - [2000]: Here first night cycle seemed to go well! Get'n taller! --- Dry again. Removed the dome. --- PH went up to 6.5 so PH'd down to 5.7 --- Ran the top feed drip ring for a bout a minute to wet the hydroton and rockwool with the nutient solution. ---Too scared to leave the top feed on 24hrs (I don't want over water her and cause dampening-off). Will let dry before re-watering. - [2100]: After closer inspection, I think she's looking a bit yellow. --- Decided to add a bit of grow nutes to the bubbler solution. --- Added 2ml of Sensi Grow A --- Added 2ml of Sensi Grow B --- Solution strength after adding more nutes: 176 PPM --- PH went up to 6 --- I hope that the extra chelating properties of the 'PH Perfect' solution is enough of a buffer for proper nutrient uptake. Day 07 - Sunday - 08/09/20 - Total Days: 007 ----------------------------------- - [0800]: Water dropped a bit (mostly due to evaporation) so solution strength was at 190. --- Checked PH again. Was still at 6, so PH'd down to 5.4 --- Ran the top feed for a minute to wet the hydroton a bit. - [0915]: Since she's looking perky but still a bit yellow. So decided to up the nutrient concentration even more before lights out. --- Added 2ml more of Sensi Grow A --- Added 2ml more of Sensi Grow B --- Solution strength after adding more nutes: 199 PPM --- PH went up to 5.8 - [1700]: Checked nutrients. --- PH: 5.9 --- Solution strength: 202 PPM --- Added 4ml of Voodoo Juice --- Added 4ml of B-52 --- PH after adding more nutes: 5.9 --- Solution strength after adding more nutes: 238 PPM - [2130]: Decided to make a new foliar spray to address the continued yellowing. --- Started with 500ml of distilled water. --- Added 3 drops of CaliMagic --- Added 3 drops of Sensi Grow A --- Added 3 drops of Sensi Grow B --- Added 3 drops of B-52 --- Added 1 drop of Superthrive --- Solution strength: 164 PPM --- PH was at 5.9 and did not adjust. --- Gave her one spray. --- Also sprayed the surrounding hydroton. [END OF WEEK 01]

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

*****Week 9 - September 14 to 20, 2020 - Days 57 to 63 from germination****** They were feeding well this week and took the higher more consistent amount of nutes well this week. Had to make a decision at the end of the week and I took out the small full spectrum light to put in the photo tent. They are in flower now and I held off as long as I can. These girls are closer to the end and I will keep the intensity focussed on LAK3 and GSC and let the other two live in the shadows and ripen😎 Not my first choice but everything is a trade off in life unfortunately☹️ Not an issue outdoor growers deal with👍 Little more detail: Sept 14/20 - Day 57 - Massive @ 3ml, Terpinator @ 2ml, Vitathrive & Liquid Weight & Rezin & Dual Fuel @ 1.5ml - 1,000ppm and 5.8pH - Feed for only LAK1......other girls area going to dry out another night. Sept 15/20 - Day 58 - Overdrive & Rezin @ 2ml, Liquid Weight & Vitathrive @ 1.5ml, Dual Fuel @ 1ml - 650ppm and 5.6pH - 2L given to each girl Sept 17/20 - Day 60 - Overdrive & Rezin @ 1.5ml - 200ppm and 5.3pH - 2L each given to the girls. - Just a bit to help with swelling. Sept 18/20 - Day 61 - Massive @ 3ml, Terpinator @ 2ml, Vitathrive & Liquid Weight & Rezin & Dual Fuel @ 1.5ml - 1165ppm and 5.2pH - LAK1 - 4L, LAK2 - 2.5L, LAK3 - 3L Sept 20/20 - Day 63 - Terpinator @ 3ml, Overdrive @ 2ml, Sensyzime & Vitathrive & Liquid Weight & Rezin & Dual Fuel @ 1.5ml - 1045ppm and 5.3pH Wrapping up week 9 and heading into week 10........the days ahead are going to be the guessing ones......is she done yet???? To be honest I have not even looked close at trichome yet🧐 I fully expect to see day 74 with LAK1.......not sure LAK2 will make it that long???? LAK3 will still be a couple of weeks yet but she is roughly a week younger. Cheers Growmies and have a great week ahead🙏😃😃😃

Everything is looking great ! Cheese is nearly done, it is starting to show amber. Maui is very happy and smells amazing, it just glistens with tri-chromes. Buttercream is doing well but I think it will take a week or two longer than the others. Blueberry is looking awesome very large thick dense buds. No Blueberry smell but a very strong plant otherwise. *Update Buttercream gelato started throwing Banana's so I removed it from the room. I trimmed it down and did not notice any other signs of hermaphroditism but I will still harvest the plant now just to be safe. There have been no issues with light or heat fluctuations at all, nothing that would trigger it to Hermie that I can think of which makes me think genetics are the issue. I have One other Buttercream going that was cloned before this one went into flower. If it hermies late in the bloom like this one has I will remove the strain from my rotation. I am not particularly pleased with the structure of Buttercream for scrog in any case. The plant that I took down had very large bud sites but were no where near as dense as the other strains in the tent.

Ginger Nut Cookies & Aussie Music Videos 13th Feb 2020 The LST seems to have been a success as the plant remains healthy and seems to be growing the way I would like it to. I'm only going to give her one more week of extra light hours with the LED, and then she can stay outside, where she can transistion into Flowering Naturally. The plant seems to have a lot of it's mothers (Fastbuds GSC) looks to it, and the stem smell when rubbed is fairly similiar too. I am still hoping for some of the Red Diesel fathers Characteristics to come thru before this girls Finished. Now for the Weekly Aussie Music Videos. Last week was a double with Yothu Yindi and Midnight Oil This week I'ts the ladies turn with a group called the Divinyls led by the charismatic Late Chrissy Amphlett who sadly passed away in 2013 from Multiple sclerosis. I cant choose between their hits "Pleasure and Pain" or " I Touch myself" so like before I'll put up the links to both Music videos Here is the Pleasure and pain link https://www.youtube.com/watch?v=5boYiMktOvs And I touch myself https://www.youtube.com/watch?v=wv-34w8kGPM I hope you enjoy this weeks diary update and Aussie music Videos Thankyou for reading this and I'll see you next Week. 👍

Added a few 6ft bamboo poles for support. She’s going to be a thick girl ❤️ She already smells pretty loud! Can’t quite describe it yet other than mouth watering.

Welcome to week 5 of flower for this lovely project! The ladies should start to put on some serious weight over the coming weeks as I've noticed most plants are done their stretch now (except macmelonz). We got lots of crazy smells coming from these plants some are harder to tell then others but some are extremely pleasing smelling already. Banana Smoothie is really putting off that banana cream smell accompanied by berries as an undertone. Creamy Cereal Crunch smells like Fruit loops and milk , its very unique and very pleasing if your into cereal anyways haha. Over all excited to see what this week will bring! Huge shout out to @MarsHydroLED for making such cool lights and tents that really make growing a breeze. Huge shout out to all my followers and people who stop into the diary alike , keep on inspiring to grow! -The Projexx Day#29F Ladies are starting to display some bulking up. Day#30F Pictures N/A. Plants seem to be stretching a bit more but concentrating on bulking up flowers. Some really nice smells coming out. Day#31F Macmelonz is still stretching along but stacking hard and the rest are starting to put on noticeable weight. Day#32F Ladies are grooving along nicely, going to look to trim up some of the middle allow for more air flow to the plants. Day#33F Banana Smoothie #1 and #4 are really starting to put out Banana Cream aromas its quite intense now. Day#34F The canopy deff needs a light defoliation. Going to defoliate slowly but surely over the coming weeks. Day#35F Pictures N/A. Ladies are really thirsty going to be upping the water next feed. Flowers are bulking like crazy! Recap: Things have gone really well this week, everyone's bulking like crazy and macmelonz who stretching out is still stacking like crazy. Lots of interesting and exciting aromas from the plants, I hope they taste as good as they smell! Over all very pleased with the performance of the plants its going to be exciting to watch them grow over the coming weeks!

Not much to update. Buds stacking nicely.

Day 14 - 3 out of 5 are growing a little slow/weird, all 5 seem to be growing kinda slow compared to my first run of autos but hopefully everything does good🤞🏼 Happy growing friends🌱✌️🏼 Day 17 - Still have 2 extremely weird looking ones, really hoping they bounce back🙏🏼🤞🏼 Day 18 - 3 out of 5 still going strong, the other 2 havnt changed much!

This week I noticed a good and healthy growth. I decided to Top one of the plants and on another one aI applied the “main line”. On the third plant from the next week I will try an “LST”. The temperature on the grow box is under control and umidity is good. The only problem we found was on the “Tangie n.2” that is developing quite slowly and showed up some yellow leafs. 20/03 we apply LTS on tangie 3 and 4.

Let plants dry out leaves started yellowing temps are very high so didn't Wana wait too long for harvest 😔

Harvested Shiva Skunk, Zombie Kush and Sweet Love.